A dominant variant in apoptosis-related gene XKR8 is relevant to hereditary auditory neuropathy

BACKGROUND: Auditory neuropathy is an unusual type of hearing loss. At least 40% of patients with this disease have underlying genetic causes. However, in many hereditary auditory neuropathy cases, etiology remains undetermined. METHODS: We collected data and blood samples from a four-generation Chi...

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Detalles Bibliográficos
Autores principales: Chen, Kaitian, Li, Changwu, Dong, Chang, Cen, Xiaoqing, Wang, Yueying, Liang, Yue, Zhu, Yuanping, Fang, Shubin, Jiang, Hongyan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131414/
https://www.ncbi.nlm.nih.gov/pubmed/37101210
http://dx.doi.org/10.1186/s12967-023-04139-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131414/
https://www.ncbi.nlm.nih.gov/pubmed/37101210
http://dx.doi.org/10.1186/s12967-023-04139-x

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